Premium
Rate constants for the addition of the 2‐hydroxy‐2‐propyl radical to alkenes in solution
Author(s) -
Héberger K.,
Fischer H.
Publication year - 1993
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.550251105
Subject(s) - chemistry , reaction rate constant , free radical addition , free radical reaction , photochemistry , radical , organic chemistry , computational chemistry , kinetics , physics , quantum mechanics
Absolute rate constants for the addition of the 2‐hydroxy‐2‐propyl radical to 18 substituted alkenes (CH 2 = C XY ) were determined at (296 ± 1) K in 2‐propanol by time‐resolved electronspin‐resonance spectroscopy. With alkene substitution the rate constants vary by more than 6 orders of magnitude. For 3,3‐dimethyl‐but‐1‐ene the temperature dependence is given by log k /M −1 · s −1 = 6.4 minus;; 19.1/Θ where Θ = 2.303 RT in kJ/mol −1 . As shown by a good correlation with the alkene electron affinities, log k 296 /M −1 · s −1 = 6.46 + 1.71 · EA/eV ( r = 0.930), 2‐hydroxy‐2‐propyl is a very nucleophilic radical, and its addition rates are highly governed by polar effects. © 1993 John Wiley & Sons, Inc.